DL-5-Fluorotryptophan

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Names

[ CAS No. ]:
16626-02-1

[ Name ]:
DL-5-Fluorotryptophan

[Synonym ]:
(S)-2-Amino-3-(5-fluoro-1H-indol-3-yl)propanoic acid
2-amino-3-(5-fluoro-1H-indol-3-yl)propanoic acid
(S)-2-AMINO-3-(5-FLUORO-1H-INDOL-3-YL)-PROPIONIC ACID
5-Fluoro-DL-tryptophan
5-Fluoro D,L-tryptophan
(2S)-2-amino-3-(5-fluoro-1H-indol-3-yl)propanoic acid
5-Fluoro-D,L-tryptophan
5-Fluorotryptophan
UNII:5IC9663SHW
Tryptophan, 5-fluoro-

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
450.7±45.0 °C at 760 mmHg

[ Molecular Formula ]:
C11H11FN2O2

[ Molecular Weight ]:
222.216

[ Flash Point ]:
226.4±28.7 °C

[ Exact Mass ]:
222.080460

[ PSA ]:
79.11000

[ LogP ]:
1.17

[ Vapour Pressure ]:
0.0±1.2 mmHg at 25°C

[ Index of Refraction ]:
1.673

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
22-24/25

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933990090

Synthetic Route

Precursor & DownStream

Precursor

  • 5-Fluoroindole
  • L-serine
  • 4-Fluoro-2-iodoaniline
  • Nα-acetyl-5-fluoro-D,L-tryptophan
  • 4-Fluoroaniline

DownStream

  • N-Fmoc-5-fluoro-L-tryptophan

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Glucose recognition proteins for glucose sensing at physiological concentrations and temperatures.

ACS Chem. Biol. 9(7) , 1595-602, (2014)

Advancements in biotechnology have allowed for the preparation of designer proteins with a wide spectrum of unprecedented chemical and physical properties. A variety of chemical and genetic methods ca...

Substrate promiscuity of the cyclic dipeptide prenyltransferases from Aspergillus fumigatus ( section sign).

J. Nat. Prod. 72 , 44-52, (2009)

This study reports that a series of tryptophan derivatives with modifications on the side chain or at the indole ring were accepted by two cyclic dipeptide prenyltransferases, CdpNPT and FtmPT1, and c...

Hydrophobic effect and hydrogen bonds account for the improved activity of a complement inhibitor, compstatin.

J. Med. Chem. 49(15) , 4616-22, (2006)

Tryptophans at positions 4 and 7 of compstatin, a peptide complement inhibitor, are crucial for its interaction with C3. However, the nature of their involvement has not been studied to date. Here we ...


More Articles


Related Compounds

  • DL-5-FLUOROTRYPTOPHAN
  • DL-5-(1,1-Dimethylethyl)-2-methoxyphenylalanine
  • DL-5-hydroxytryptophane amide
  • DL-5-Bromo-2-methoxyphenylalanine
  • DL-5-(3,4-dimethoxybenzyl)hydantoin
  • DL-5-bromotryptophan methyl ester
  • 3-(4-Fluoro-2-methylphenyl)-3-methylbutanoic acid
  • 3-(2,3-Difluorophenyl)-3-methylbutanoic acid
  • N-[1-(Aminocarbonyl)-3-hydroxy-3-methylbutyl]benzamide
  • 6-bromo-N-(thiazol-2-yl)benzo[d]thiazol-2-amine
  • 3-Methyl-3-(2-methylpropyl)oxirane-2-carbonitrile
  • 3-Hexyl-3-methyloxirane-2-carbonitrile
  • 1-Oxaspiro[2.11]tetradecane-2-carbonitrile
  • 3-(1-ethyl-1H-pyrazol-4-yl)-3-methylbutanoic acid
  • 3-Methyl-3-(6-methylpyridin-3-yl)butanoic acid
  • 3-Methyl-3-(2,3,4-trifluorophenyl)butanoic acid